Supplementary Figures 1 - 3 from <i>max</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Nelly Burnichon , Alberto Cascón , Francesca Schiavi , Nicole Paes Morales , Iñaki Comino‐Méndez , Nasséra Abermil , Lucía Inglada-Pérez , Aguirre A. de Cubas , Laurence Amar , Marta Barontini , Sandra Bernaldo de Quirós , Jérôme Bertherat , Yves‐Jean Bignon , Marinus J. Blok , Sara Bobisse , Salud Borrego , Maurizio Castellano , Philippe Chanson , María‐Dolores Chiara , Eleonora P.M. Corssmit , Mara Giacchè , Ronald R. de Krijger , Tonino Ercolino , Xavier Girerd , Encarna B. Gómez-García , Álvaro Gómez-Graña , Isabelle Guilhem , Frederik J. Hes , Emiliano Honrado , Esther Korpershoek , Jacques W.M. Lenders , Rocío Letón , Arjen R. Mensenkamp , Anna Merlo , Luigi Mori , Arnaud Murat , P. Pierre , Pierre‐François Plouin , Tamara Prodanov , Miguel Quesada‐Charneco , Nan Qin , Elena Rapizzi , Victoria M. Raymond , Nicole Reisch , Giovanna Roncador , Macarena Ruiz‐Ferrer , F. Schillo , Alexander P.A. Stegmann , Carlos Suárez , Elisa Taschin , Henri Timmers , Carli M.J. Tops , Miguel Urioste , Felix Beuschlein , Karel Pacák , Massimo Mannelli , Patricia L. M. Dahia , Giuseppe Opocher , Graeme Eisenhofer , Anne‐Paule Gimenez‐Roqueplo , Mercedes Robledo openalex
摘要
PDF file, 794KB, Supplementary figure S1. Gross MAX deletion analysis Supplementary figure S2. Immunohistochemical assessment. Supplementary figure S3. Pedigree of 3 families with affected relatives in more than one generation.
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